Moura Lucio Roberto Requião, Tonato Eduardo José, Ferraz Érika Arruda, Filliponi Thiago Corsi, Chinen Rogério, Matos Ana Cristina Carvalho, Silva Maurício Rodrigues Fregonesi da, Durão Marcelino de Souza, Pacheco-Silva Alvaro
Hospital Israelita Albert Einstein, São Paulo, SP, BR.
Einstein (Sao Paulo). 2011 Mar;9(1):56-65. doi: 10.1590/S1679-45082011AO1838.
To compare three different regimens of thymoglobulin induction.
One hundred seventy two patients submitted to renal transplantation from a dead donor were divided into three groups according to the total number of thymoglobulin doses used in the post-transplantation surgery: Group 1, until 14 doses - May 2002 to June 2004 (n = 48); Group 2, until 7 doses - July 2004 to December 2006 (n = 57); Group 3, until 4 doses - January 2007 to July 2009 (n = 67). The three groups were compared according to the main outcomes.
The main demographic differences among the groups were: greater dialysis time in Group 3 (p < 0.001 for Group 1; and p = 0.04 for Group 2); donor age, greater in Groups 2 and 3 (p = 0.02; p = 0.01, respectively); and cold ischemia time progressively greater from Group 1 to 3: 19.5 ± 5.1 to 24.6 ± 5.7 hours (p < 0.001). In relation to the inhibitor of calcineurin, the relation Tac/Csa was 14.6/66.7% in Group 1, 78.9/12.3% in Group 2 and 100/0% in Group 3. Reflecting the increase in cold ischemia time, the incidence of delayed graft function was 64.6%, 68.4% e 82.1% in Groups 1, 2 and 3, respectively (p = ns). The incidence of acute rejection was similar in the three groups: 16.7% (1); 16.3% (2) and 16.4 (3) - p = ns. The prevalence of viremia for cytomegalovirus was 61.7% in Group 1, 66.1% in Group 2 and 83.3% in Group 3 (p = ns). There were no difference related to the number of infected cells with cytomegalovirus in antigenemia, according to the groups, however, patients in Group 3 had an earlier diagnosis: from 64.3 ± 28.5 days in Grup 2, to 47.1 ± 22.5 days, in Group 3, p < 0.001. Survival of the graft in one year was 89.6%, 92.9% and 91.0%, in Groups 1, 2 and 3, respectively (p = ns). The graft function was much better with the lower doses of thymoglobulin: Group 1: 57.0 ± 20.0 mL/min; Group 2: 67.0 ± 18.4 mL/min (p = 0.008); Group 3: 71.2 ± 18.4 mL/min (p < 0.001, Group 1 versus Group 3; p = 0.06, Group 1 versus Group 2). There was a significant reduction in the costs of induction protocol from U$ 7,567.02 to U$ 3,485.56 (p < 0.001).
The total number of thymoglobulin doses for immunologic induction could be reduced in a safe and effective way, without a negative impact in graft rejection or survival, preserving renal function and being significantly cheaper.
比较三种不同的抗胸腺细胞球蛋白诱导方案。
172例接受死体供肾移植的患者,根据移植术后使用抗胸腺细胞球蛋白的总剂量分为三组:第1组,直至14剂 - 2002年5月至2004年6月(n = 48);第2组,直至7剂 - 2004年7月至2006年12月(n = 57);第3组,直至4剂 - 2007年1月至2009年7月(n = 67)。根据主要结局对三组进行比较。
各组间主要人口统计学差异为:第3组透析时间更长(与第1组相比p < 0.001;与第2组相比p = 0.04);供体年龄,第2组和第3组更大(分别为p = 0.02;p = 0.01);冷缺血时间从第1组到第3组逐渐增加:19.5 ± 5.1至24.6 ± 5.7小时(p < 0.001)。关于钙调神经磷酸酶抑制剂,第1组中他克莫司/环孢素的比例为14.6/66.7%,第2组为78.9/12.3%,第3组为100/0%。反映冷缺血时间增加,第1、2和3组移植肾功能延迟的发生率分别为64.6%、68.4%和82.1%(p = 无统计学意义)。三组急性排斥反应的发生率相似:16.7%(第1组);16.3%(第2组)和16.4%(第3组) - p = 无统计学意义。巨细胞病毒血症的患病率在第1组为61.7%,第2组为66.1%,第3组为83.3%(p = 无统计学意义)。根据组间比较,抗原血症中巨细胞病毒感染细胞数量无差异,然而,第3组患者诊断更早:从第2组的64.3 ± 28.5天,到第3组的47.1 ± 22.5天,p < 0.001。三组移植肾1年生存率分别为89.6%、92.9%和91.0%(p = 无统计学意义)。抗胸腺细胞球蛋白剂量越低,移植肾功能越好:第1组:57.0 ± 20.0 mL/分钟;第2组:67.0 ± 哪.4 mL/分钟(p = 0.008);第3组:71.2 ± 18.4 mL/分钟(第1组与第3组相比p < 0.001;第1组与第2组相比p = 0.06)。诱导方案的成本从7567.02美元显著降低至3485.56美元(p < 0.001)。
免疫诱导的抗胸腺细胞球蛋白总剂量可以安全有效地减少,对移植肾排斥反应或存活无负面影响,可保护肾功能且成本显著降低。